| dc.creator |
KÜÇÜKGÜVEN, ARDA |
|
| dc.creator |
Aydin, Asim |
|
| dc.creator |
Ozgur, Figen |
|
| dc.creator |
Canter, Halil Ibrahim |
|
| dc.creator |
VARGEL, İBRAHİM |
|
| dc.date |
2022-05-01T00:00:00Z |
|
| dc.identifier |
65af1f24-ccba-46b4-85e5-54c447740f3b |
|
| dc.identifier |
10.1177/10556656211019621 |
|
| dc.identifier |
https://avesis.sdu.edu.tr/publication/details/65af1f24-ccba-46b4-85e5-54c447740f3b/oai |
|
| dc.description |
Aim: The term frontonasal dysplasia (FND) represents a spectrum of anomalies and its genetics have not been well defined. Recently, the critical role of the aristaless-like homeobox (ALX) gene family on the craniofacial development has been discovered. In the present study, we aimed to propose a systematic surgical treatment plan for the ALX-related FNDs according to the genotypic classification as well as demonstrating their clinical characteristics to help surgeons diagnose the underlying pathology accurately. |
|
| dc.language |
eng |
|
| dc.rights |
info:eu-repo/semantics/closedAccess |
|
| dc.title |
ALX-Related Frontonasal Dysplasias: Clinical Characteristics and Surgical Management |
|
| dc.type |
info:eu-repo/semantics/article |
|